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Your search keyword '"Chen, Chih‐Ling"' showing total 12 results
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3. Prenatal diagnosis of 9q34.3 microdeletion-associated Kleefstra syndrome in a pregnancy complicated by polyhydramnios: A case report and literature review

Author

Tai, Yi-Yun, Chen, Chih-Ling, Wu, Chen-Tu, Lee, Chien-Nan, and Lin, Shin-Yu

Abstract

Kleefstra Syndrome (KS) is a rare genetic disorder caused by a deletion at 9q34.3. Studies showed that various heart defects are observed in 41–43% of patients and abnormal features on brain imaging in 58–63%. To date, the prenatal phenotype in KS has yet to be defined.

Published
2024
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7. Additional file 1 of Cobalt protoporphyrin promotes human keratinocyte migration under hyperglycemic conditions

Author

Fang, Peng-Hsiang, Lai, Ying-Ying, Chen, Chih-Ling, Wang, Hsin-Yu, Chang, Ya-Ning, Lin, Yung-Chang, Yan, Yu-Ting, Lai, Cheng-Hung, and Cheng, Bill

Subjects
integumentary system
Abstract

Additional file 1. Fig. S1. Schematic diagram showing the live-cell imaging protocol of CoPP treated HaCaT underwent migration in either normal glucose or high glucose media. Fig. S2. The influence of CoPP on the motility of WS1 in in vitro wound healing assay. Fig. S3. Quantitative analysis of the protein expressions in CoPP-pretreated HaCaT cultured in either NG or HG media. Fig. S4. Quantitative analysis of the protein expressions in CoPP-treated WS1 cultured in either NG or HG media. Fig. S5. Viability of CoPP-pretreated HaCaT cultured in either normal glucose or high glucose in the presence of 300 µM H2O2. Fig. S6 Schematic diagram showing the live-cell imaging protocol of CoPP pretreated HaCaT cultured in either low glucose or high glucose after H2O2 exposure. Fig. S7. Viability of HaCaT cultured in LPS-containing media

Published
2022
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12. First report of a successful pregnancy by preimplantation genetic testing for Beckwith-Wiedemann syndrome

Author

Yang, Ih-Jane, Tu, Yi-An, Pan, Song-Po, Huang, Ting-Chi, Chen, Chih-Ling, Lin, Ming-Wei, Tsai, Yi-Yi, Yao, Yi-Lin, Su, Yi-Ning, and Chen, Shee-Uan

Abstract

Beckwith-Wiedemann syndrome (BWS) is a rare imprinting gene disorder. Maternal CDKN1Cmutation comprises 5% of etiologies of BWS. There is no successful report of preventing BWS by preimplantation genetic testing for monogenic disease (PGT-M) in the literature. Is PGT-M applicable for preventing BWS ?

Published
2021
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